Canonical Allele Identifier: PA2827971860
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2816057
ClinVar RCV Id: RCV003744141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val2626Asp
CA16038599
NM_001354898.2:c.7877T>A